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Acute isoniazid neurotoxicity in an urban hospital

B R Shah1, K Santucci, R Sinert

  • 1Department of Pediatrics, Children's Medical Center of Brooklyn, State University of New York 11203-2098, USA.

Pediatrics
|May 1, 1995
PubMed

Insights

Acute isoniazid (INH) neurotoxicity increased with tuberculosis resurgence. Children presenting with seizures, especially with INH exposure, should be evaluated for toxicity. Prompt pyridoxine administration is crucial for managing INH-induced seizures.

Area of Science:

  • Pediatric Neurology
  • Toxicology
  • Infectious Disease Epidemiology

Background:

  • Tuberculosis (TB) resurgence in urban centers has led to increased use of isoniazid (INH) for prophylaxis and treatment.
  • Acute isoniazid neurotoxicity is a rare but serious adverse effect, particularly in pediatric populations.
  • Understanding the presentation and management of INH neurotoxicity is crucial for timely diagnosis and intervention.

Observation:

  • A case series identified seven pediatric patients treated for acute INH neurotoxicity between 1991 and 1993, contrasting with zero cases from 1985-1990.
  • This increase paralleled a rise in pediatric TB cases at the institution, from 96 to 213 annually.
  • Patients presented with seizures, often afebrile, following accidental ingestion or intentional overdose of INH.

Findings:

  • The mean ingested dose was 54 mg/kg (range 14.3-99.3 mg/kg).
  • Two patients with refractory seizures required parenteral pyridoxine for control after failing anticonvulsant therapy.
  • Diagnostic delay occurred due to INH neurotoxicity not being initially suspected.

Implications:

  • Increased incidence of acute INH neurotoxicity is linked to the resurgence of TB.
  • Pediatricians and emergency departments should maintain a high index of suspicion for INH toxicity in children with seizures, especially with known INH exposure.
  • Parenteral pyridoxine should be readily available in emergency departments to manage INH-induced seizures effectively.
Abstract

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